Skip to search formSkip to main contentSkip to account menu

PRKD2 wt Allele

Known as: HSPC187, PKD2, DKFZP586E0820 
Human PRKD2 wild-type allele is located in the vicinity of 19q13.3 and is approximately 43 kb in length. This allele, which encodes serine/threonine… 
National Institutes of Health

Related topics

Related topics

5 relations
19q13.3PhosphorylationSerine/Threonine PhosphorylationSignal Transduction

Broader (1)

PRKD2 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2018
Review
2018
Antenatally Diagnosed ADPKD
2015
2015
The PKD Inhibitor CID755673 Enhances Cardiac Function in Diabetic db/db Mice
The development of diabetic cardiomyopathy is a key contributor to heart failure and mortality in obesity and type 2 diabetes… 
2015
2015
PKD2 and RSK1 Regulate Integrin β4 Phosphorylation at Threonine 1736
The integrin α6β4, a major component of hemidesmosomes (HDs), stabilizes keratinocyte cell adhesion to the epidermal basement… 
2013
2013
Lysophosphatidic acid-stimulated phosphorylation of PKD2 is mediated by PI3K p110β and PKCδ in myoblasts
Abstract Context: G-protein coupled receptor (GPCR) signaling in skeletal muscle is incompletely understood; in particular, the… 
2011
2011
Protein kinase Cδ mediates the activation of protein kinase D2 in platelets.
Highly Cited
2008
Highly Cited
2008
PKD, PKD2, and p38 MAPK mediate Hsp27 serine‐82 phosphorylation induced by neurotensin in pancreatic cancer PANC‐1 cells
It is widely recognized that Hsp27 is a downstream substrate of the p38 MAPK cascade whereas the role of PKD family members in… 
2006
2006
PKD2 gene mutation analysis in Korean autosomal dominant polycystic kidney disease patients using two‐dimensional gene scanning
Autosomal dominant polycystic kidney disease (ADPKD) is genetically heterogeneous and is caused by mutations in the PKD1 or PKD2… 
2003
2003
Structural requirements for subcellular localisation of the novel serine threonine kinase PKD2 in human gastric cancer cells
1997
1997
DNA diagnosis and clinical manifestations of autosomal dominant polycystic kidney disease.
At least 2 genes, detectable by DNA methods, encode autosomal dominant polycystic kidney disease (ADPKD), which remains the most… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)